50-198-8780

TRPM5 Rabbit anti-Human, Polyclonal, Bioss

Manufacturer: Bioss

Select a Size

Pack Size SKU Availability Price
Each of 1 50-198-8780-Each-of-1 In Stock ₹ 38,381.25

50-198-8780 - Each of 1

₹ 38,381.25

In Stock

Quantity

1

Base Price: ₹ 38,381.25

GST (18%): ₹ 6,908.625

Total Price: ₹ 45,289.875

Antigen

TRPM5

Classification

Polyclonal

Conjugate

Unconjugated

Gene

trpm5

Gene Alias

9430099A16Rik; Long transient receptor potential channel 5; long transient receptor potential-related channel 5; LTRPC5; LTrpC-5; MLSN1 and TRP-related; MLSN1- and TRP-related gene 1 protein; MTR1; si:dkey-56p7.1; Transient receptor potential cation channel subfamily M member 5; transient receptor potential cation channel, subfamily M, member 5; transient receptor potential melastatin 5; TRPM5

Host Species

Rabbit

Purification Method

Protein A

Regulatory Status

RUO

Gene ID (Entrez)

29850

Content And Storage

-20°C

Form

Liquid

Applications

Immunofluorescence, Immunohistochemistry (Paraffin), Western Blot

Concentration

1 μg/mL

Formulation

PBS with 1% BSA, 50% glycerol and 0.09% sodium azide; pH

Gene Accession No.

Q9NZQ8

Gene Symbols

trpm5

Immunogen

KLH conjugated synthetic peptide derived from human TRPM5.

Quantity

100 μL

Primary or Secondary

Primary

Target Species

Human

Product Type

Antibody

Isotype

IgG

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Description

  • This gene encodes a member of the transient receptor potential protein family, which is a diverse group of proteins with structural features typical of ion channels
  • This protein plays an important role in taste transduction, and has characteristics of a calcium-activated, non-selective cation channel that carries Na+, K+, and Cs+ ions equally well, but not Caions
  • It is activated by lower concentrations of intracellular Ca, and inhibited by higher concentrations
  • It is also a highly temperature-sensitive, heat activated channel showing a steep increase of inward currents at temperatures between 15 and 35 degrees Celsius
  • This gene is located within the Beckwith-Wiedemann syndrome critical region-1 on chromosome 11p15
  • 5, and has been shown to be imprinted, with exclusive expression from the paternal allele.